Multi-layer films of block copolymer micelles adsorbed to colloidal templates

Author(s):  
Timothy Addison ◽  
Olivier J. Cayre ◽  
Simon Biggs ◽  
Steven P. Armes ◽  
David York

Alternating layers of cationic and anionic block copolymer micelles have been deposited onto colloidal silica particles using a layer-by-layer approach. The resulting films have been investigated using a number of characterization techniques including zeta potential measurements, dynamic light scattering, thermo-gravimetric analysis and microscopy. The micelles used here demonstrate pH-responsive behaviour both in solution and when adsorbed at interfaces. It has been shown that block copolymer micelles can selectively encapsulate and release hydrophobic materials; therefore, the incorporation of such responsive species within films has the potential to offer increased functionality. The formation of films onto colloidal particles is of great interest as it can provide pathways to direct encapsulation of materials along with surface modification. This study aims to provide new insights into the nature and properties of responsive films. Such studies will allow for the future development of novel delivery systems that have potential application within a number of industrial sectors including personal care products, pharmaceuticals and agro-chemicals.

2018 ◽  
Vol 51 (9) ◽  
pp. 3467-3476 ◽  
Author(s):  
Anbazhagan Palanisamy ◽  
Svetlana A. Sukhishvili

2014 ◽  
Vol 5 (12) ◽  
pp. 3777-3787 ◽  
Author(s):  
Pelin Yusan ◽  
Irem Tuncel ◽  
Vural Bütün ◽  
A. Levent Demirel ◽  
Irem Erel-Goktepe

2007 ◽  
Vol 19 (23) ◽  
pp. 5524-5530 ◽  
Author(s):  
Phuong M. Nguyen ◽  
Nicole S. Zacharia ◽  
Eric Verploegen ◽  
Paula T. Hammond

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yan Cui ◽  
Hongyan Zhu ◽  
Jiandong Cai ◽  
Huibin Qiu

AbstractControlled self-assembly of colloidal particles into predetermined organization facilitates the bottom-up manufacture of artificial materials with designated hierarchies and synergistically integrated functionalities. However, it remains a major challenge to assemble individual nanoparticles with minimal building instructions in a programmable fashion due to the lack of directional interactions. Here, we develop a general paradigm for controlled co-assembly of soft block copolymer micelles and simple unvarnished hard nanoparticles through variable noncovalent interactions, including hydrogen bonding and coordination interactions. Upon association, the hairy micelle corona binds with the hard nanoparticles with a specific valence depending exactly on their relative size and feeding ratio. This permits the integration of block copolymer micelles with a diverse array of hard nanoparticles with tunable chemistry into multidimensional colloidal molecules and polymers. Secondary co-assembly of the resulting colloidal molecules further leads to the formation of more complex hierarchical colloidal superstructures. Notably, such colloidal assembly is processible on surface either through initiating the alternating co-assembly from a micelle immobilized on a substrate or directly grafting a colloidal oligomer onto the micellar anchor.


2011 ◽  
Vol 355 (1) ◽  
pp. 61-69 ◽  
Author(s):  
Irem Erel ◽  
Zhichen Zhu ◽  
Aliaksandr Zhuk ◽  
Svetlana A. Sukhishvili

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